Photoisomerization of Azobenzene‐Extended Charybdotoxin for the Optical Control of K<sub>v</sub>1.2 Potassium Channel Activity

Natural peptides from animal venoms effectively modulate ion channel activity. While photoswitches regulate small compound pharmacology, their application to natural peptides rich in disulfide bridges and active on ion channels is novel due to larger pharmacophores. A pilot study integrating azobenzene photoswitches into charybdotoxin (ChTx), known for blocking potassium channels is initiated. Two click-chemistry-compatible azobenzene are synthesized differing in length and amide orientation (Az<sub>1</sub> & Az<sub>2</sub>). Az<sub>1</sub> is grafted onto ChTx at various amino acid positions using L-azidohomoalanine mutation. ChTx monomers outperformed dimers, particularly with azobenzene at position 14, by exhibiting optimal photoswitching activity. In the cis configuration, Az<sub>1</sub> altered ChTx's pharmacophore, reducing potassium channel blockage, while conversely, Az<sub>2</sub> increased ChTx potency. This study pioneers photoswitch application to complex peptides, leveraging structure-activity relationships. Successful integration depends on precise azobenzene positioning and chemical grafting guided by SAR insights. This advancement underscores the adaptability of photoswitch technology to intricate peptide structures, offering new avenues for pharmacological modulation.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-03-09
DOI
https://doi.org/10.1002/anie.202423278
Citations
5
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
2.59

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article

Photoisomerization of Azobenzene‐Extended Charybdotoxin for the Optical Control of Kv1.2 Potassium Channel Activity

Cécile Caumes, Éléna Ishow, Hervé Meudal, Heike Wulff et al.
5 citations
Angewandte Chemie International Edition
Luminescence and Fluorescent Materials
2.59
article

Photoisomerization of Azobenzene‐Extended Charybdotoxin for the Optical Control of Kv1.2 Potassium Channel Activity

Cécile Caumes, Éléna Ishow, Hervé Meudal, Heike Wulff, Michel De Waard, Basile Pérès, Stéphane Téletchéa, Ahcène Boumendjel, Steven Ascoët, Mikaël Croyal, Céline Landon, Hugo Millet, Claude Zoukimian, Jérôme Montnach, Rémy Béroud, Yanis Achouba, Fella Bouchama, Maureen Choteau‐Bodor, Cathy Carvalhosa
article en
5 citations

Abstract

Natural peptides from animal venoms effectively modulate ion channel activity. While photoswitches regulate small compound pharmacology, their application to natural peptides rich in disulfide bridges and active on ion channels is novel due to larger pharmacophores. A pilot study integrating azobenzene photoswitches into charybdotoxin (ChTx), known for blocking potassium channels is initiated. Two click-chemistry-compatible azobenzene are synthesized differing in length and amide orientation (Az<sub>1</sub> & Az<sub>2</sub>). Az<sub>1</sub> is grafted onto ChTx at various amino acid positions using L-azidohomoalanine mutation. ChTx monomers outperformed dimers, particularly with azobenzene at position 14, by exhibiting optimal photoswitching activity. In the cis configuration, Az<sub>1</sub> altered ChTx's pharmacophore, reducing potassium channel blockage, while conversely, Az<sub>2</sub> increased ChTx potency. This study pioneers photoswitch application to complex peptides, leveraging structure-activity relationships. Successful integration depends on precise azobenzene positioning and chemical grafting guided by SAR insights. This advancement underscores the adaptability of photoswitch technology to intricate peptide structures, offering new avenues for pharmacological modulation.

Angewandte Chemie International EditionVol. 64(19)
Institut polytechnique de Grenoble (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Département de Chimie Moléculaire (FR), Centre de Biophysique Moléculaire (FR), Chimie et Interdisciplinarité, Synthèse, Analyse, Modélisation (FR), Institut du Thorax (FR), Institute of Molecular Biology and Biophysics (RU), Peptide Institute (Japan) (JP), Laboratoire d'Excellence Canaux Ioniques d'Intérêt Thérapeutique (FR), Thorax Foundation (GR), Chemical Synthesis Lab (SG), University of California, Davis (US), Université Grenoble Alpes (FR), Nantes Université (FR)
Agence Nationale de la Recherche, Fondation Leducq, Conseil Régional des Pays de la Loire
Openalex Percentile: Top 11%
Luminescence and Fluorescent Materials
2.59
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